Thin Cell Layer (TCL) Culture System for Herbal Biomass Production and Genetic Transformation of Bacopa monnieri L. Wettst.


Bacopa monnieri (L.) Wettst. (Scrophulariaceae) is a highly sought after medicinal plant with therapeutic properties as cognition enhancer as well as for other brain and body functions. Research was conducted to optimize a thin cell layer explant based micropropagation system to assist mass propagation. Thin cell layers (TCL) derived from leaf and internode segments were used as explants. Murashige and Skoog medium was used to formulate shoot induction, elongation, and rooting media. Shoot induction media were prepared by supplementing three concentrations (0.1, 1.0, and 10.0 μM) of four cytokinins 6-benzylaminopurine, 2-isopentenyl-adenine, 6-3-Hydroxybenzylaminopurine, and thidiazuron to study adventitious shoot bud induction response. An optimum shoot bud induction response was observed on MS medium supplemented with 10.0 μM 6-benzylaminopurine for both leaf and stem transverse thin cell layer (tTCL) explants. The average number of shoot buds from leaf tTCL explants was 59, whereas, on an average, 33 shoot buds were regenerated from internode tTCL explants. Elongation of adventitious shoot buds was achieved best in a liquid medium using Liquid Lab Rocker® system. Elongated shoots recorded 100% rooting in MS medium supplemented with 5 μM indole butyric acid. Bacopa micropropagation employing tTCL explants for initial shoot bud induction and using LLR® boxes in subsequent elongation step can achieve cost effective way to regenerate high volume of plantlets and biomass required for herbal industry. Leaf and stem tTCL explants both were suitable for Agrobacterium tumefaciens (EHA105) mediated genetic transformation. Successful transformation was scored within three days of co-cultivation with Agrobacterium suspension on the basis of Enhanced Green Fluorescent Protein (EGFP) expression as an early and non-destructible screening device. Transformation frequencies of 83% and 76% were accomplished for leaf and stem tTCL explants, respectively. Greenhouse grown Bacopa plants were analyzed as fresh and dry methanolic extracts for total polyphenol content (811.93 ± 7.98 and 814 ± 17.64 GAE mg g-1) and the Trolox Equivalent Antioxidant Capacity values were 1918.25 ± 173.12 and 3163.14 ± 403.25 μmol/g, respectively.

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Croom, L. , Jackson, C. , Vaidya, B. , Parajuli, P. and Joshee, N. (2016) Thin Cell Layer (TCL) Culture System for Herbal Biomass Production and Genetic Transformation of Bacopa monnieri L. Wettst.. American Journal of Plant Sciences, 7, 1232-1245. doi: 10.4236/ajps.2016.78119.

Received 18 May 2016; accepted 14 June 2016; published 17 June 2016

1. Introduction

Bacopa monnieri (L.) Wettst. (Bacopa monniera, family Scrophulariaceae) is a well-documented herb in the traditional Ayurveda medical system attributed with medicinal properties improving cognition, such as memory retention, concentration, and learning [1] . Though Bacopa (locally known as Brahmi) is indigenous to India, it has been found in wild in countries as far away as Argentina [2] . In a few research communications, ecological status of this important herb in wild has been mentioned as endangered one [3] . In many countries, Bacopa species are also commercially sold as an aquatic plant for the aquarium. Flowers and fruits appear in summer and the entire plant is used for medicine. The bioactivity and medicinal properties have been assigned to the presence of alkaloids (nicotine, brahmine, herpestine), saponins (hersaponin, betulic acid, bacosides A, B, C and D) and other chemicals like stigmastanol, bsitosterol and stigmasterol [4] - [6] . Clinical studies have further evaluated the nootropic potential of Bacopa monnieri and confirmed its cognition-enhancing effects, attributing the effects to bioactive compounds collectively known as “bacosides” [7] . Bacosides are a type of saponin triterpene, and the bioactive compounds Bacosides A and B aid in the repair of damaged neurons by enhancing kinase activity, neuronal synthesis, restoration of synaptic activity, and ultimately, nerve impulse transmission [8] .

Though there are a few reports on the micropropagation of Bacopa monnieri [9] [12] - [14] , a thorough study to maximize plant production with minimum tissue requirement for initial explant is lacking. To ensure large scale commercial production of biomass for herbal industry, it would be pertinent to bring down the cost of production. Significant cost reduction can be achieved with liquid culture system [10] [11] .

Further, most of the regeneration studies conducted earlier on Bacopa are restricted to the use of cytokinins such as kinetin, BAP [12] [13] and TDZ [14] - [18] . Recent regeneration studies in Spathiphyllum floribundum Schott cv. Petite and Hisbiscus sabdariffa L. a compound with cytokinin like activity known as meta-Topolin shows promising results [19] [20] . Other cytokinins like 2-iP can also induce adventitious bud induction in Bacopa either using individually or in combination with an auxin [21] . Thin cell layer (TCL) culture system is one of the options to ensure minimal use of tissue as an explant. By definition, thin cell layer culture is the use of small explants (width: 0.1 mm to 1 mm and length: 5 - 10 mm) [22] . Depending on the incision made, an explant can either be longitudinal or transverse thin cell layer (l or tTCL). As a result of their reduced size, more cells within a thin cell layer explant are “morphogenically responsive” due to their close contact with the growth medium [22] . The effects of cytokinins, auxins, photoperiod, on successful regeneration and biolistic or bacterial-mediated transformation have been reported in species such as Nicotiana tabacum, Lilium longiflorum, Lycopersicon esculentum, Dendranthema x grandiflora, Eclipta alba, Orchids and various species of Rose thin cell layer cultures [23] - [28] . There are no reported studies that evaluate the effects of cytokinins on thin cell layer (TCL) explants of B. monnieri for improved and efficient plant production. Recent advances in metabolic engineering have made it possible to increase the concentration of desired compounds as well as introduce novel biosynthetic pathways leading into the production of novel bioactive compounds [29] [30] . To improve metabolic engineering capabilities, it is important to have an efficient in vitro multiplication protocol in place. Genetic transformation studies that have been carried out in Bacopa genus so far have been summarized in Table 1. This study seeks to optimize adventitious shoot bud induction to facilitate herbal biomass production, role of liquid culture in shoot elongation, rooting and genetic transformation potential of tTCL explants.

Table 1. A review of genetic transformation research on Bacopa monnieri.

2. Materials and Methods

2.1. Transverse Thin Cell Layer Culture (tTCL) of B. monnieri

2.1.1. Preparation of Plants for Mother Stock

Bacopa plants that were growing in the greenhouse were sterilized using a procedure optimized in our lab [16] . After sterilization nodal explants were established as in vitro cultures on Murashige and Skoog (MS) medium [31] with vitamins (PhytoTechnology Lab, KS, USA). These plants were allowed to grow for four weeks in test tubes with 15 mL culture medium under 16 h photoperiod at 24˚C ± 2˚C, and then used for harvesting explants for all the experiments.

2.1.2. Explant Selection

Plant materials were harvested from the aseptic mother stock maintained on MS basal medium. The leaf and stem tTCL explants were aseptically excised using surgical blade No. 11 (Feather, Osaka, Japan) from axenic mother cultures of B. monnieri, to achieve the desired sizes. Using fully expanded in vitro leaf and internode stem tissues, tTCL explants were prepared. The average initial tTCL leaf explant dimensions were less than 3 mm in length and 1 mm in width and the stem explant dimensions were about 1.5 - 2.0 mm in diameter and 1.0 - 1.5 mm in thickness.

2.1.3. Media and Culture Conditions for Multiple Adventitious Shoot Induction

MS medium with vitamins was fortified with 3% (w/v) sucrose and 0.8% (w/v) agar (Caisson Labs, UT, USA). This medium was used to observe the rate of multiple shoot induction from using leaf and internode tTCLs explant by incorporating three concentrations of four cytokinins or compounds with cytokinins like activity.

Three concentrations 0.1µM, 1.0 µM, and 10 µM, each of four cytokinins viz. 6-benzylaminopurine (BAP) (PhytoTechnology Lab, KS, USA), 2-isopentenyl-adenine (2-iP) (Sigma Aldrich, MO, USA), meta-Topolin (m-Topolin) (PhytoTechnology Lab, KS, USA), and Thidiazuron (TDZ) (Sigma Aldrich, MO, USA), and a control containing no plant growth regulators, were incorporated into MS medium. The pH was adjusted to 5.8 before autoclaving at 121˚C for 15 minutes. The sterilized media was dispensed into sterile plastic Petri dishes (100 mm × 15 mm; Fisher Scientific, MA, USA) and allowed to solidify in the sterile condition at 25˚C. Five leaf and five stem tTCL explants were inoculated in each petri dish and three petri dishes for each treatment were inoculated.

2.2. Elongation, Rooting, and Acclimatization in Greenhouse

After 14 days of incubation in the initial shoot induction medium with various cytokinins, explants with adventitious shoot buds were transferred to the elongation medium to induce further shoot growth. Liquid MS basal medium with 1% sucrose was used as elongation medium and 40 mL of it was dispensed in each LLR® box. Five tTCL explants (either leaf or stem) with multiple shoot buds were transferred to each LLR® box. These cultures were incubated at 25˚C ± 2˚C for two weeks. Once healthy root system was visible, plants were removed from the LLR® boxes and washed under tap water to remove medium and sucrose. Plants with clean roots were transferred to plastic pots containing potting mixture (Promix BX, Premier Tech Horticulture, PA, USA) and placed under the mist chamber for acclimatization. Plants were then removed from the mist chamber after a week and maintained in the greenhouse to monitor further growth.

2.3. Scanning Electron Microscopy

Samples were processed through fixation, dehydration, critical point drying and sputter coating prior to analyzing adventitious shoot bud induction under scanning electron microscope (S 3400N II, Hitachi High Technologies America Inc., CA, USA). The protocol followed has been optimized in our lab and published earlier [32] . The gold coating was at 50 Å. Coating was carried out for 60 s under a vacuum pressure of 0.05 torr using 30 mA current. Digital images were collected at various magnifications running beam at 10 kV and keeping specimen stub at 4.4 mm distance. All scanning works were conducted at the Agricultural Research Station, Fort Valley State University, Fort Valley, Georgia, USA.

2.4. Agrobacterium tumefaciens-Mediated Genetic Transformation of tTCL Explants

The standard protocol for Agrobacterium tumefaciens-mediated transformation of B. monnieri leaf and stem tTCL cultures was optimized testing the following parameters―choice of explants, bacterial suspension preparation, acetosyringone concentration added to the bacterial culture prior to co-cultivation, and co-cultivation time. Agrobacterium tumefaciens EHA 105 competent cells previously prepared and stored at −80˚C were transformed with plasmid (pq35SGR, 14469 bp; kindly provided by Dr. Dennis J Gray, University of Florida). This plasmid contains EGFP, GUS/NPTII fusion reporter genes and the plasmid harboring bacteria was cultured in 2YT plates with 20 mg/L rifampicin (Sigma Aldrich, MO, USA), and 50 mg/L kanamycin (Sigma Aldrich, MO, USA) antibiotics. The plates were then incubated in the dark at 28˚C for 48 - 72 h. Once the clean, isolated, and single conspicuous colonies were visible, they were picked to initiate new cultures. A single colony was selected to prepare bacterial culture for co-cultivation.

2.4.1. Co-Cultivation of tTCL Explants

Agrobacterium culture was placed in incubator (27˚C) at 160 RPM for further growth. After 24 h, 3 mL of Agrobacterium culture was mixed with 23 mL of MG/L medium with 20 mg/L rifampicin and 50 mg/L Kanamycin [33] in 50 mL falcon tubes (BD, NJ, USA), and placed back in the incubator (Amerex Instruments, Inc., CA, USA) for growth. Optical density (OD) of Agrobacterium culture was measured at 600 nm using spectrophotometer (Nanodrop 2000c; Thermo Scientific, MA, USA) after 24 h. Once the bacterial culture OD600 reaches between 0.4 and 0.6, 100 µM of acetosyringone (Phyto Technology Laboratories, KS, USA) was added to the bacterial culture and was further incubated for 2 h. The shoot and leaf tTCLs were transferred to sterile petri dish (Fisher Scientific, MA, USA) with 10 mL of Agrobacterium culture suspension for 25 min. Explants were placed in the bacterial suspension for 25 min and the suspension was swirled occasionally to provide explant cut surface for attachment of Agrobacterium. After 25 min of co-cultivation, explants were removed from the bacterial suspension and excess bacterial solution was removed by blotting explants on a sterile filter paper. The tTCL explants were placed in petri dish containing sterile filter paper and 3 mL of liquid MS medium was used to keep explants moist and maintain high humidity required for agro-infection. The petri dishes were wrapped with Parafilm® (American National Can Co., CT, USA), placed in incubator (27˚C) for 48 h. After 48 h, the explants were blotted to remove excess Agrobacterium on sterile tissue paper and placed in washing solution containing liquid MS medium supplemented with 1 µM BAP, 250 mg/L cefotaxime (Caisson Lab, UT, USA) and 250 mg/L carbenicillin (Caisson Lab, UT, USA). After washing explants for three hours in washing solution, cultures were transferred to semi-solid MS medium with 2.5 µM BAP, 250 mg/L cefotaxime (Caisson Lab, UT, USA) and 250 mg/L carbenicillin. The explants were observed daily under UV light for EGFP expression (Olympus SZX12 with DP 71 camera; Olympus, PA, USA) in developing adventitious shoots, other organs and tissues. Transformation of 25 leaf and stem tTCL explants was repeated three times to score transformation frequency.

2.4.2. Selection of Putative Transformants

The transformed stem and leaf tTCL explants were selected on MS based shoot induction medium containing 30 mg/L kanamycin. Cultures were incubated under 16 h photoperiod at 25˚C. After 30 days on the selection medium, only the kanamycin resistant tTCL leaf and stem explants survived that developed into shoots when transferred to fresh optimized regeneration medium (MS + 3% sucrose, 10 µM BAP, 250 mg/L carbenicillin, 250 mg/L cefotaxime, and 30 mg/L kanamycin). Developing adventitious shoots were regularly examined for EGFP expression and once elongating shoots expressed GFP uniformly, they were also evaluated utilizing the histochemical GUS assay [34] employing β-Glucuronidase reporter gene staining Kit (Sigma-Aldrich, MO, USA). Chlorophyll was removed from the putative transgenic tissue by passing it through 2 - 3 changes of 70% ethanol and the blue stain developed was photographed as outlined by the manufacturer.

2.4.3. Molecular Characterization of Putative Transgenic Plants

Reverse Transcription-Polymerase Chain Reaction (RT-PCR) Analysis

Total RNA from non-transgenic and transgenic Bacopa plants were extracted from the leaves using a modified TRIzol® reagent (Ambion/Life Technologies, NY, USA) method. RNA quantification was done using a NanoDrop 2000c Spectrophotometer (Thermo Scientific, MA, USA). RT-PCR was performed with 600 ng of RNA using a One Taq® One-Step RT-PCR Kit (New England Biolabs Inc., MA, USA). Reverse transcription was conducted in PCR tubes at 48˚C for 30 min, followed by initial denaturation at 94˚C for one min, and 40 cycles of denaturation at 94˚C for 15 s, annealing at 65˚C for 30 s, and extension at 68˚C for 1 min. Final extension was carried out at 68˚C for 5 min. The negative control consisted of the same reaction samples described above except for the absence of the One Taq® One-Step enzyme. Equal amount (400 ng) of control and experimental cDNAs were used as template for performing PCR. A forward primer EG-51 (50-ATG GTGAGCAAGGGCGAGGAGCTGT-30) and a reverse primer EG-32 (50-CTTGTACAGCTCGTCCATGCCG AGA-30) were used to amplify the egfpgene. The RT-PCR products were analyzed using 1.0% (w/v) agarose stained with GelRedTM (Biotium, CA, USA).

2.5. Antioxidant Capacity Measurement of B. monnieri Leaves

Extracts Preparation, Total Polyphenol (TPP) Content Measurement and TROLOX Equivalent Antioxidant Capacity (TEAC) Assay

Tissue processing and extract preparation was carried out as described earlier [35] . In brief, liquid nitrogen was used to grind 2 g of fresh and dried whole plant samples of B. monnieri in a chilled mortar and pestle. The ground tissues were extracted overnight (14 h) in dark at 25˚C using 50 mL methanol (Burdick and Jackson, MI, USA) using orbital shaker (Benchmark Mini Incushaker, NJ, USA) at 200 RPM. Extracts were centrifuged at 8000 × g (Eppendorf centrifuge 5810 R; NY, USA) for 15 min and supernatant were collected in a 50 mL clean tubes (Corning, NY, USA). The pellets in the tubes were further extracted two more times for 30 min each in 50 mL methanol. All extracted fractions were combined and passed through a 0.2 µm nylon filter (Nalgene, NY, USA) before storage and downstream processing. The TPP experiments were carried out in quadruplicate and the mean TPP values for both fresh and dried plant extract of B. monnieri were quantified as µg/g Gallic Acid Equivalents (GAE).

Total polyphenol content (TPP) was determined by the Folin-Ciocalteu reagent method [36] ; and antioxidant capacity measurement was determined using TROLOX Equivalent Antioxidant Capacity (TEAC) assay [37] with modification [38] . Rosemary (Rosmarinus officinalis) leaf extracts were used as the internal standard to compare antioxidant capacity. The absorption values were recorded at 765 nm with Nanodrop 2000c spectrophotometer (Thermo Scientific, MA, USA) for both assays after standard curves were generated.

2.6. Statistical Analysis

The shoot induction experiments were carried out in triplicate for each treatment. A total of 15 explants from each type (leaf and stem tTCL) were used to score data. Once the optimum medium was identified, the same preparations were carried out in triplicate to record the shoot induction of the tTCL cultures. The experiments were set up in completely randomized design and repeated three times. A one-way Analysis of Variance (ANOVA) between subjects was conducted to compare the effect of type of cytokinin and concentration on shoot induction for B. monnieri’s tTCL leaf and stem explants with results at P < 0.05 level. The significant means were separated using Tukey’s post-hoc mean separation test. All data are presented as means ± SE for each sample.

3. Results

3.1. Organogenesis Using tTCL of B. monnieri

Adventitious Shoot Organogenesis and Elongation

A preliminary investigation was carried out to test the suitability of MS and Gamborg’s B5 medium [39] for tTCL based micropropagation. Employing visual observations like explant establishment, response time, explant necrosis and browning, and number of shoot buds generated during first four weeks of culture, MS medium proved more suitable. Subsequent experiment on adventitious shoot bud induction using tTCL explants were carried out by supplementing MS based medium with three concentrations of four cytokinins as outlined above. Another preliminary study supported by qualitative observations revealed that the inclusion of auxin NAA even at 0.1 µM resulted in the development of multiple roots (data not presented). As our interest is multiple shoot induction, auxin NAA was omitted from shoot induction media treatments. Morphogenic response of leaf and stem tTCL explants has been shown in the Figure 1. In this experiment, MS supplemented with 10 µM BAP resulted

Figure 1. Various stages in adventitious shoot bud induction of B. monnieri leaf tTCL. (a) tTCL at day 1; (b) tTCL at 10 day; (c) tTCL at 14 day. Various stages in adventitious shoot bud induction of B. monnieri stem tTCL. (d) tTCL at day 1; (e) tTCL at 10 day; (f) tTCL at 14 day; (g) tTCL at 21 day. Various stages in elongation and rooting of B. monnieri leaf and stem tTCL in LLR system. (h) Utilization of LLR system to mass propagate B. monnieri after shoot bud induction in liquid MS medium; (i) A vigorously growing clump of elongated shoots of B. monnieri leaf tTCL after transferred to LLR boxes; (j) Rooted shoots of B. monnieri plantlet ready to be transferred to potting medium; (k)-(l) Sequence of callus induction and adventitious shoot production on the stem tTCL of Bacopa; (m) A single adventitious shoot in detail.

in the best response for adventitious shoot bud induction from leaf (59) as well as stem (33) tTCL explants (Figure 2). Among all the cytokinins used, 2-iP exhibited poorest response as at 0.1 µM level no shoot bud induction was visible, as did the control treatment with no cytokinin (Figure 2). Explants were transferred to liquid MS basal mediums with 1% sucrose after 14 day exposure on shoot induction medium to ensure elongation of shoots (Figure 1(c) and Figure 1(g)). Elongated shoots were removed from the elongation medium after three weeks and were photographed to record shoot length and root induction (Figure 1(i)). BAP treatment at 10 µM scored 879 shoots in total from 15 tTCL explantsafter a 14 day incubation producing highest shoot count for leaf tTCL. Other treatments like 0.1 µM of m-Topolin only had 24 shoots and 0.1 µM of 2-iP did not produce any shoots at all. The average numbers of shoots harvested from the most favorable treatment for leaf tTCL was 59 shoots per explant (Figure 1(i) and Figure 2). Overall, leaf tTCL explants produced more adventitious shoot buds when compared to stem tTCLs.

To carry out liquid medium assisted elongation, culture assembly used is shown in the Figure 1(h). Culture boxes receive light from top and bottom both and are gently rocked (10 times/minute). Bacopa shoots elongated rapidly and a clump of elongated shoot generating from tTCL explant looks like Figure 1(i). It is interesting to note that shoots elongated rapidly and some of the clumps that received lower levels of cytokinins concentration rooted as well (Figure 1(j)). Another notable feature of elongation phase was no incidence of hyperhydricity in Bacopa shoots.

3.2. Root Induction and Elongation

Two to three cm long Bacopa monnieri shoots resulted in the establishment of well-developed root systems when transferred to semi-solid MS basal medium supplemented with 1% sucrose and 0.7% agar. Majority of shoots rooted in this medium. Addition of 5 µM Indole-3-butyric acid (IBA) (PhytoTechnology Lab, KS, USA) into MS basal medium, resulted in higher number of shoots striking roots within a shorter incubation time (7 - 10 days) [16] .

Figure 2. Adventitious shoot bud induction on leaf and stem tTCL explants of B. monnieri in response to various cytokinin treatments. Each mean and ± SE is based on three replicates of fifteen explants. Means having different superscript alphabets are significantly different from each other (p < 0.05).

3.3. Agrobacterium tumefaciens-Mediated Genetic Transformation of tTCL Explants

The latest reported studies on Agrobacterium tumefaciens-mediated transformation report efficient, rapid, and simple protocols with the highest transformation frequency being reported at 68.8% [40] - [47] . The reporter genes β-glucuronidase and neomycin phosphotransferase are the two genes that have been used in prior research [42] [43] . There are no reports that evaluate the Agrobacterium tumefaciens-mediated transformation of tTCL B. monnieri. The EGFP protein expression proved to be very effective in selecting transiently expressed tTCL leaf and stem explants, to be moved to selection medium and later elongated (Figures 3(a)-(c)). After three independent studies for both the tTCL leaf and tTCL stem explants a transformation frequency of 83% and 76% was accomplished respectively (data not presented).

3.3.1. GUS Analysis of Transgenic Cultures and Plants

Transient GUS expression was determined from explants five days after co-cultivation, whereas stable GUS expression in transgenic cultures and plants was recorded after three months of co-cultivation using manufacturer’s instructions.

3.3.2. RT-PCR Analysis of GFP Transcript

Using the primers outlined in the Materials and Methods section, an approximately 774 bp, single band was amplified (Figure 4). This corresponds to PCR generated fragment using the same primers on genomic DNA isolated from putative transgenic plant (data not shown).

3.4. Antioxidant Studies of B. monnieri Leaves

The Folin-Ciocalteu reagent method and TROLOX Equivalent Antioxidant Capacity (TEAC) assay was utilized to analyze the total polyphenol content (TPP) and antioxidant capacity of B. monnieri herb. The Gallic Acid Equivalent (GAE) values were 811.93 ± 7.98 mg/g and 814 ± 17.64 mg/g, for the fresh and dried methanolic extracts of B. monnieri providing a measure of total flavonoids. The TEAC values 1918 ± 173.12 µmol/g and 3163.14 ± 403.247 µmol/g (Table 2), for the fresh and dried plant extracts of B. monnieri indicate this plant to possess high antioxidant capacity.

Figure 3. EGFP observation. (a) Transformed tTCL stem explant exhibiting GFP expression five days after co-cultivation; (b) Transgenic, GFP positive shoot bud induction on a tTCL stem explant 10 days after co-cultivation; (c) Adventitious rooting on tTCL stem explant 21 days after co-cultivation. Histochemical GUS Assay observation; (d) Normal leaf serves as control for GFP and GUS activity both; (e) Results of histochemical staining process in leaf.

Figure 4. PCR studies on wild type and putative transgenic plant. The RT-PCR products were analyzed using 1.0% (w/v) agarose. M: 100 bp DNA step ladder (Promega), C: Control with No cDNA in the reaction, WT: Wild type plant, PT: Putative transgenic. Arrow indicates single amplified band for egfp gene.

Table 2. Total polyphenol content and TEAC assay of fresh and dried whole plants of Bacopa monnieri.

*Values given are means and ± SE of four replicates. Means having different superscripts are significantly different from each other as per the Tukey’s HSD test (p < 0.05).

4. Discussion

Bacopa extracts have been extensively used in Indian Ayurvedic medicinal system for a number of human disorders including inflammation, pain, epilepsy, ulcer, and most importantly, for improving cognitive and other brain functions [8] [48] [49] . Mechanisms of cognitive and brain enhancement include its anti-oxidative activities [50] as well as modulation of the cholinergic system [51] [52] . Moreover, upregulation of neuronal and glial plasticity [53] and beta-amyloid scavenging activities [6] have also been reported. Among various pre-clinical reports for biological activities, the memory, attention or cognitive enhancing effect of Bacopa extracts have been confirmed by several double-blinded, placebo-controlled human clinical studies (reviewed by Pase et al. [49] ). An ongoing randomized clinical trial to study the effect of Bacopa extract CDR1 08 on Attention Deficit Hyperactivity Disorder (ADHD) in children and adolescents has been reported [54] , results of which are awaited.

The goal of this study was to develop and optimize protocols for in vitro adventitious shoot induction for B. monnieri using tTCL explants to raise commercially acceptable plant production with equal or better biological activity. This research is further optimization of our findings that were reported earlier [16] . We focused on optimizing the use of explant, choice of cytokinin and medium condition to develop a rapid multiplication system. It is interesting to note that tTCL explants need only two weeks on shoot induction medium in this protocol and elongate well within three weeks on liquid culture. There are no prior studies reporting multiple shoot induction using tTCL culture method for B. monnieri explants, or evaluating the effects of meta-Topolin (m-Topolin). However, high number of shoot induction in MS medium supplemented with 1.1 µM BAP + 0.2 µM IAA, resulting in 110 shoots from a single normal leaf explants was reported [13] . We have previously reported that increasing concentrations of BAP (0.1, 0.5, and 1.0 mg/L) had a positive effect on the number of shoots produced - inducing 13, 13, and 6 shoots respectively [12] . These differences could be due to the use of different genotype in the experiment. In vitro mass multiplication of B. monnieri using MS medium supplemented with 1.0 µM of BAP was the best medium producing 41 shoots on a normal leaf explant [9] . Current study also supports the superiority of MS medium for shoot bud induction and elongation. Earlier report on organogenesis from normal Bacopa explants using leaves and internodes on different concentrations of BAP and 2,4-D showed that 0.5 mg/L BAP and 0.5 mg/L 2,4-D produced highest number of shoots [16] . Cytokinin such as BAP in concentration of 6 µM has shown to have high frequency of shoot bud regeneration from leaf explants [39] . Previous reports show that adventitious shoots can be regenerated from internodes using various concentrations of BAP and NAA [35] . In this study, meta-Topolin proved as an effective cytokinin, though not the best one (Figure 2). In case of S. barbata, and S. racemosa at the 14 and 21 day incubation periods meta-Topolin proved as the most effective cytokinin. Utilization of the LLR® system over semi-solid medium can decrease the cost of production since agar is not used in the medium (Figures 1(h)-(j)), as well as the amount of time for roots to be successfully induced. Using this method, in vitro generated plantlet’s transition for acclimatization is more efficient as all excess medium-derived nutrients and sucrose can be rinsed off with running tap water more effectively than with semi-solid medium.

We have earlier reported the success of micropropagating transverse versus longitudinal sections of B. monnieri [16] . However, these sections were not small enough to qualify as “thin cell layers”. The mean length and width of a Bacopa leaf is 8.61 mm × 27.00 mm. One will be able to generate over thirty tTCL leaf explants from a single leaf, and utilizing the media preparation found in this study will be able to produce up to 59 plantlets per tTCL. In an optimized protocol, more than 1829 plantlets can be produced in one cycle from one leaf, which is far more than previous reports. When compared to previous studies using normal sized explants, the high number of shoots induced on such a thin layer of cells from the leaf and stem Bacopa explants, supersedes total shoots induced from one leaf or one internode explant [9] [13] . Given this research is focused on the optimization of multiple shoot induction, we completely omitted the use of a low level of auxin in the shoot induction medium as it resulted in rooting. The utilization of the LLR® system over semi-solid medium during elongation phase seems to have positive effects in that the omission of agar results in decreasing the cost of production, early root initiation, and plants are agar free for hardening process, bringing down the mortality rate. As there was no hyperhydricity case observed, scaled up liquid culture system can be an ideal technology for Bacopa mass production. As there is no need to orient explants in specific manner, and hood time taken by culturist is decreased resulting in higher productivity.

The transformation frequency utilizing leaf and stem tTCL explants correlates with past studies suggesting it to be a viable option [42] [55] . To study semi-quantitative analysis of the transgene at mRNA level, RT-PCR is a reliable technique. Leaf and stem tTCL explants both were suitable for transformation.

High TPP and TEAC values correlate with previously reported pre-clinical studies showing that this medicinal herb is effective in combating oxidative stress [50] [56] . A preliminary study on the antioxidant potential and total polyphenol content of this plant was also carried out during this research. As per recent studies that have evaluated the benefits of phenols and antioxidants against oxygen radicals and non-free radical species that cause oxidative stress, it is necessary to quantify the total polyphenol content (TPP) and antioxidant potential of the B. monnieri species [57] . Volluri et al. (2011) [58] reported 27.76 ± 1.87 mg/gm GAE and Prasad et al. (2012) [59] reported 58 mg/g GAE TPP for B. monnieri. Solvents do affect the total phenolic content and antioxidant potential as the highest TPP, DPPH radical scavenging activity, and superoxide anion radical scavenging activities were reported with methanolic extracts as compared to hexane, petroleum ether, and water [60] . Previous studies report the TPP of B. monnieri whole plant in other conventional solvents, hexane, petroleum ether, water, and methanol, as 59.1, 88.0, 107.5, and 241.3 µg GAE/g respectively [60] . Only methanolic extracts were measured in this study. The means of TPP for the fresh and dried greenhouse B. monnieri were 811.93 ± 7.98 and 814.37 ± 17.64 mg/g GAE (Table 1). These numbers are the highest for fresh and dried TPC reported so far for B. monnieri. This study reports much higher GAE and TEAC values than prior studies [56] [59] . It can be concluded from this study, that the protocol utilized for in vitro micropropagation of B. monnieri is at this point a better choice in terms of economics and product turnover. The antioxidant protocol is especially useful in setting the baseline for future studies.


LAC and CLJ thank for Graduate Research Assistantship provided through “Strengthening the Minority Serving Institutions Project” (FVSU Project # 331079, Dr. Nirmal Joshee, PD/PI) entitled “Advancing Graduate Education in the STEM Disciplines for the Underserved African American and Low Income American Population” funded by the United States Department of Education.


*Corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.


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